These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 38881794)

  • 41. Clinical features of MELAS and its relation with A3243G gene point mutation.
    Zhang J; Guo J; Fang W; Jun Q; Shi K
    Int J Clin Exp Pathol; 2015; 8(10):13411-5. PubMed ID: 26722549
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature.
    Gagliardi D; Mauri E; Magri F; Velardo D; Meneri M; Abati E; Brusa R; Faravelli I; Piga D; Ronchi D; Triulzi F; Peverelli L; Sciacco M; Bresolin N; Comi GP; Corti S; Govoni A
    Front Neurol; 2019; 10():38. PubMed ID: 30766507
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes-MELAS Syndrome.
    Henry C; Patel N; Shaffer W; Murphy L; Park J; Spieler B
    Ochsner J; 2017; 17(3):296-301. PubMed ID: 29026367
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A novel tRNA(Val) mitochondrial DNA mutation causing MELAS.
    Tanji K; Kaufmann P; Naini AB; Lu J; Parsons TC; Wang D; Willey JZ; Shanske S; Hirano M; Bonilla E; Khandji A; Dimauro S; Rowland LP
    J Neurol Sci; 2008 Jul; 270(1-2):23-7. PubMed ID: 18314141
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Familial mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode syndrome: Three case reports.
    Yang X; Fu LJ
    World J Clin Cases; 2022 Sep; 10(27):9945-9953. PubMed ID: 36186180
    [TBL] [Abstract][Full Text] [Related]  

  • 46. MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNA
    Kuwajima M; Goto M; Kurane K; Shimbo H; Omika N; Jimbo EF; Muramatsu K; Tajika M; Shimura M; Murayama K; Kurosawa K; Yamagata T; Osaka H
    Brain Dev; 2019 May; 41(5):465-469. PubMed ID: 30739820
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes in an older adult mimicking cerebral infarction: a Chinese case report.
    Fang GL; Zheng Y; Zhang YX
    Clin Interv Aging; 2018; 13():2421-2424. PubMed ID: 30568433
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Independent origin for m.3243A>G mitochondrial mutation in three Venezuelan cases of MELAS syndrome.
    Florez I; Pirrone I; Casique L; Domínguez CL; Mahfoud A; Rodríguez T; Rodríguez D; De Lucca M; Ramírez JL
    Clin Biochem; 2022; 109-110():98-101. PubMed ID: 36130631
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Unique presentation of LHON/MELAS overlap syndrome caused by m.13046T>C in MTND5.
    Kolarova H; Liskova P; Tesarova M; Kucerova Vidrova V; Forgac M; Zamecnik J; Hansikova H; Honzik T
    Ophthalmic Genet; 2016 Dec; 37(4):419-423. PubMed ID: 26894521
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Renal involvement in MELAS syndrome - a series of 5 cases and review of the literature.
    Seidowsky A; Hoffmann M; Glowacki F; Dhaenens CM; Devaux JP; de Sainte Foy CL; Provot F; Gheerbrant JD; Hummel A; Hazzan M; Dracon M; Dieux-Coeslier A; Copin MC; Noël C; Buob D
    Clin Nephrol; 2013 Dec; 80(6):456-63. PubMed ID: 22909780
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Design and use of a peptide nucleic acid for detection of the heteroplasmic low-frequency mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) mutation in human mitochondrial DNA.
    Hancock DK; Schwarz FP; Song F; Wong LJ; Levin BC
    Clin Chem; 2002 Dec; 48(12):2155-63. PubMed ID: 12446471
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an
    Zheng H; Zhang X; Tian L; Liu B; He X; Wang L; Ding S; Guo Y; Cai J
    Front Neurosci; 2022; 16():1028762. PubMed ID: 36685235
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Autopsied case with MERRF/MELAS overlap syndrome accompanied by stroke-like episodes localized to the precentral gyrus.
    Miyahara H; Matsumoto S; Mokuno K; Dei R; Akagi A; Mimuro M; Iwasaki Y; Yoshida M
    Neuropathology; 2019 Jun; 39(3):212-217. PubMed ID: 30972844
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Identification of a Novel Variant in
    Xu M; Kopajtich R; Elstner M; Wang Z; Liu Z; Wang J; Prokisch H; Fang F
    Front Genet; 2021; 12():638749. PubMed ID: 34054915
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Comprehensive Diagnostic Criteria for MELAS Syndrome; a Case Study Involving an Elderly Patient With MT-TWm.5541C>T Mutation.
    Wu G; Shen Y; Zhu F; Tao W; Zhou Y; Ke S; Jiang H
    Neurologist; 2023 May; 28(3):190-194. PubMed ID: 36125978
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Epilepsy Characteristics and Clinical Outcome in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS).
    Lee HN; Eom S; Kim SH; Kang HC; Lee JS; Kim HD; Lee YM
    Pediatr Neurol; 2016 Nov; 64():59-65. PubMed ID: 27671241
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Adult onset MELAS Syndrome Presenting as A Mimic of Herpes Simplex Encephalitis.
    Chen WT; Lin YS; Wang YF; Fuh JL
    Acta Neurol Taiwan; 2019 Jun; 28(2)():46-51. PubMed ID: 31867706
    [TBL] [Abstract][Full Text] [Related]  

  • 58. An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA.
    Terauchi A; Tamagawa K; Morimatsu Y; Kobayashi M; Sano T; Yoda S
    Brain Dev; 1996; 18(3):224-9. PubMed ID: 8836506
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.
    Wang YX; Le WD
    Chin Med J (Engl); 2015 Jul; 128(13):1820-5. PubMed ID: 26112726
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) mtDNA mutation that induces subacute dementia which mimicks Creutzfeldt-Jakob disease.
    Isozumi K; Fukuuchi Y; Tanaka K; Nogawa S; Ishihara T; Sakuta R
    Intern Med; 1994 Sep; 33(9):543-6. PubMed ID: 8000105
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.